5'-EthylcarboxaMido-2',3'-isopropylidene Adenosine

5'-EthylcarboxaMido-2',3'-isopropylidene Adenosine Structure
CAS No.
39491-53-7
Chemical Name:
5'-EthylcarboxaMido-2',3'-isopropylidene Adenosine
Synonyms
2’,3’-O-isopropylidene-NECA;5'-ETHYLCARBOXAMIDO-2',3'-ISOPROPYLIDENEADENOSINE;5'-Ethylcarboxamido-2',3'-O-isopropylideneadenosine;1-(6-Amino-9H-purin-9-yl)-1-deoxy-N-ethyl-2,3-O-(1-methylethylidene)--D-ribofuranuronamide;b-D-RibofuranuronaMide,1-(6-aMino-9H-purin-9-yl)-1-deoxy-N-ethyl-2,3-O-(1-Methylethylidene)-;β-D-Ribofuranuronamide, 1-(6-amino-9H-purin-9-yl)-1-deoxy-N-ethyl-2,3-O-(1-methylethylidene)-
CBNumber:
CB5648971
Molecular Formula:
C15H20N6O4
Molecular Weight:
348.3571
MOL File:
39491-53-7.mol
MSDS File:
SDS
Modify Date:
2023/5/3 8:29:06

5'-EthylcarboxaMido-2',3'-isopropylidene Adenosine Properties

Melting point 200-202°C
Density 1.69±0.1 g/cm3(Predicted)
solubility DMSO, Ethanol, Methanol
form Solid
pka 14.47±0.60(Predicted)
color Pale Yellow

5'-EthylcarboxaMido-2',3'-isopropylidene Adenosine Chemical Properties,Uses,Production

Chemical Properties

Pale Yellow Solid

Uses

As a useful template for the development of A2B adenosine receptor agonists, 5'-EthylcarboxaMido-2',3'-isopropylidene Adenosine was confirmed to be a full agonist in a functional assay based on the measurement of its capacity to modulate cAMP levels in CHO cells expressing the hA2B receptor.

5'-EthylcarboxaMido-2',3'-isopropylidene Adenosine Preparation Products And Raw materials

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39491-53-7(5'-EthylcarboxaMido-2',3'-isopropylidene Adenosine)Related Search:

5'-ETHYLCARBOXAMIDO-2',3'-ISOPROPYLIDENEADENOSINE 1-(6-Amino-9H-purin-9-yl)-1-deoxy-N-ethyl-2,3-O-(1-methylethylidene)--D-ribofuranuronamide 2’,3’-O-isopropylidene-NECA 5'-Ethylcarboxamido-2',3'-O-isopropylideneadenosine b-D-RibofuranuronaMide,1-(6-aMino-9H-purin-9-yl)-1-deoxy-N-ethyl-2,3-O-(1-Methylethylidene)- β-D-Ribofuranuronamide, 1-(6-amino-9H-purin-9-yl)-1-deoxy-N-ethyl-2,3-O-(1-methylethylidene)- 39491-53-7 C15H20N6O4 Bases & Related Reagents Carbohydrates & Derivatives Heterocycles Nucleotides